Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:154121293-154121430 | Common:2; Rare:61 | ||||
chr3:155079835-155079904 | Rare:22 | ||||
chr3:155854355-155854763 | Rare:111 | ||||
chr3:155870323-155870706 | Common:2; Rare:114 | ||||
chr3:156674373-156674618 | Common:3; Rare:67 | ||||
chr3:157160101-157160295 | Rare:83 | ||||
chr3:157543230-157543435 | Rare:44 | ||||
chr3:158105732-158105878 | Common:5; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
chr3:158110023-158110156 | Rare:29 | ||||
chr3:158571022-158571200 | Common:1; Rare:52 | ||||
chr3:158801871-158802168 | Common:3; Rare:113 | ||||
chr3:160399196-160399307 | Rare:30; Clinvar:1 | ||||
chr3:160399514-160399669 | Rare:34 | ||||
chr3:161221229-161221326 | Rare:29 | ||||
chr3:169773313-169773429 | Rare:39 |